This reaction involves phenol, chloroform (\( \text{CHCl}_3 \)), and sodium hydroxide (\( \text{NaOH} \)) to form salicylaldehyde, which is an example of the Reimer-Tiemann reaction.
1. Step 1: Understand the Reimer-Tiemann reaction.
- The Reimer-Tiemann reaction is used to introduce a formyl group (–CHO) onto the benzene ring of phenols, typically using chloroform and a strong base like sodium hydroxide.
2. Step 2: The mechanism.
- In this reaction, phenol reacts with chloroform in the presence of sodium hydroxide to form an intermediate dichlorocarbene, which then reacts with the phenol to form the salicylaldehyde.
Thus, the reaction is known as the Reimer-Tiemann reaction.